Nitrogen Contents and Isotopic Characteristics of Mesozoic and Cenozoic Granites in Northeastern China

The method of determining the nitrogen isotopic composition of granites in the northeastern part of China is described.The content and isotopic values of nitrogen released from granite samples by stepwise heating were determined as well.The results showed that the diferent areas of northeastern China hae a great difference in nitrogen content and isotopic composition.Nitrogen released from the granites is 1.64-6.23μL/g ,with the maximum at about 600℃,from rhyolite and granophyre is 108.98-755.96μL/g,with the maximum at about 900℃,It is proved that fluid is characterized by heterogeneity in the deep crust of the different areas in northeastern China.The nitrogen isotopic compositions in different ranges of temperautes are wweighted.And the nitrogen isotopic compositions in different anges of temperatures are weighted.And the nitrogen isotopic values are 9.2‰ to 17.0‰,with a variation range of 7.8‰,The nitrogen isotopic ratios may have been fractionated during degassing and the fluid released from granites is the residual component.     

Comparative Study of Hydrogen and Carbon Isotopic Composition of Gases Generated from the Pyrolysis of a Peat under Saltwater and Freshwater Conditions

To understand the influence of the diagenetic water medium on the isotopic compositions of thermogenic coalbed gas, both hydrous and anhydrous closed-system pyrolyses were performed at temperatures of 250°C to 650°C on an herbaceous marsh peat. Compared to the results of anhydrous pyrolysis, the hydrocarbon gases generated from hydrous pyrolyses have very different hydrogen isotopic compositions. However, the carbon isotopic compositions of the hydrocarbon gases became only slightly heavier in hydrous pyrolysis, compared to that from anhydrous pyrolysis. With the progress of thermal evolution from peat to a more advanced thermal maturity of vitrinite reflectance values (Ro) of 5.5% during the pyrolysis, the difference in the average δD value increased from 52‰ to 64‰ between the hydrous pyrolysis with saltwater and anhydrous pyrolysis and increased from 18‰ to 29‰ between the hydrous pyrolysis with freshwater and anhydrous pyrolysis, respectively. The difference in the average δ13C value was only 1‰–2‰ between the hydrous and anhydrous pyrolysis. The relationships between the δD values of the generated hydrocarbon gases and Ro values as well as among δD values of the hydrocarbon gas species are established. The close relationships among these parameters suggest that the water medium had a significant effect on the hydrogen isotopic composition and a minimal effect on the carbon isotopic composition of the hydrocarbon gases. The results of these pyrolyses may provide information for the understanding of the genesis of coalbed gas from herbaceous marsh material with the participation of different diagenetic water media.     

Composition and Evolution of Hydrogen Isotopes of n-Akanes Generated from Anhydrous Pyrolysis of Sediments from Lake Gahai,Gannan, China

To understand the thermal evolution of lacustrine sedimentary n-alkane hydrogen isotopic composition (δD), especially bacterially derived n-alkanes, anhydrous thermal simulation experiments were performed with sediments from Lake Gahai (Gannan, China). We analyzed the original and pyrolysis-generated n-alkanes and their δD values. The results showed that thermal maturity and n-alkane origins significantly affected the distribution of pyrolysis-generated n-alkanes. In immature to post-mature sediments, the bacterial-derived medium-chain n-alkanes generally had depleted δD values. The maximum difference in average δD values between the bacterial-and herbaceous plant-derived medium-chain n-alkanes was 32‰, and the maximum difference in δD values among individual n-alkanes was 59‰. We found that the average δD value of pyrolysis-generated n-alkanes from different latitude was significantly different in immature to highly mature sediments, but similar in post-mature ssediments. The hydrogen isotopes of sedimentary n-alkanes can be used as indicators for paleoclimate/paleo-environment conditions only when sediments are immature to highly mature. During thermal evolution, the δD value of generated individual n-alkanes and the average δD value increased with thermal maturity, indicating that hydrogen isotopes of sedimentary n-alkanes can be used as an index of organic matter maturity. We established mathematical models of average δD values of generated n-alkanes from immature to post-mature sediments using nC21?/nC21+ and average chain lengths. These results improve our understanding of the distribution and δD value of sedimentary n-alkanes derived from herbaceous plants in mid-latitude plateau cold regions.     

Hydrogen isotope of individual n-alkanes from modern sediments and their application to environments

Hydrogen isotopes are commonly fractionated to a much greater extent and as a result display larger variations in δ values, In terms of the hydrogen isotope ratios of individual n-alkanes of 16 samples of modern sediments selected from four different locations in the southern part of Gansu, China, the δD values for most of the n-alkanes varied from -150‰-300‰, Variations in δD also occurred between different ranges of n-alkanes, effects of environmental changes on the hydrogen isotopic compositions of individual n-alkanes have been detected. Besides the δD values of n-alkanes, the δD values of lipids including pristane （Pr）, phytane （Ph） were also examined, by the combination of D/H ratios with molecular fingerprinting, Our results further support the notion that hydrogen isotopes of n-alkanes from modern sediments can act as paleoclimatic and paleoenvironmental proxies and provide invaluable new sources of information in the research of paleoenvironment reconstruction.     

Carbon and oxygen isotopic composition of car- bonate cements of different phases in terrigenous siliciclastic reservoirs and significance for their origin： A case study from sandstones of the Triassic Yanchang Formation, southwestern Ordos Basin, China

Early carbonate cements in the Yanchang Formation sandstones are composed mainly of calcite with relatively heavier carbon isotope （their δ^18O values range from -0.3‰- -0.1‰） and lighter oxygen isotope （their δ^18O values range from -22.1‰- -19.5‰）. Generally, they are closely related to the direct precipitation of oversaturated calcium carbonate from alkaline lake water. This kind of cementation plays an important role in enhancing the anti-compaction ability of sandstones, preserving intragranular volume and providing the mass basis for later disso- lution caused by acidic fluid flow to produce secondary porosity. Ferriferous calcites are characterized by relatively light carbon isotope with δ^13C values ranging from -8.02‰ to -3.23‰, and lighter oxygen isotope with δ^18O values ranging from -22.9‰ to -19.7‰, which is obviously related to the decarboxylation of organic matter during the late period of early diagenesis to the early period of late diagenesis. As the mid-late diagenetic products, ferriferous cal- cites in the study area are considered as the characteristic authigenic minerals for indicating large-scaled hydrocarbon influx and migration within the clastic reservoir. The late ankerite is relatively heavy in carbon isotope with δ^13C values ranging from -1.92‰ to -0.84‰, and shows a wide range of variations in oxygen isotopic composition, with δ^18O values ranging from -20.5‰ to -12.6‰. They are believed to have nothing to do with decarboxylation, but the previously formed marine carbonate rock fragments may serve as the chief carbon source for their precipitation, and the alkaline diagenetic environment at the mid-late stage would promote this process.     

Genetic classification of natural gases in the Bozhong Depression, Bohai Bay, China

The geochemical characteristics of natural gases discovered in the Bozhong Depression are systematically described in this paper. The natural gases are composed mainly of hydrocarbon gases. Natural gases occurring in the Paleogene and older reservoirs are wet gases, whereas those in the Neogene reservoirs are dry gases. Methane and ethane in the gases are significantly different in carbon isotopic composition. The methane carbon isotopic composition of the gases in structure BZ28-1 and the ethane carbon isotopic composition of the gases in structure QHD30-1 are characterized by the heaviest values, respectively. The natural gases are in the mature to highly mature stages. The hydrocarbon gases are of organic origin and can be classified as oil-type gases, coal-derived gases and mixed gases with the third one accounting for the major portion.     

Carbon Isotopic Evolution of the Late Ediacaran Gaojiashan Biota on the Northern Yangtze Platform,South China

Metazoan fossils in the Gaojiashan Biota are famous for being well preserved and may provide new insights into the early evolution and skeletonization of Metazoans. We are studying the isotopic compositions of organic and carbonate carbon from a sequence of sedimentary rocks at the Gaojiashan section, northern Yangtze Platform, Shaanxi Province of China. Organic carbon isotope values display a range between –30.8‰ and –24.7‰ with clear stratigraphic variations. Carbonate carbon isotope data vary between 0.1‰ and +6‰. Positive δ13C values from sediments with Gaojiashan biota reflect temporal variations in carbon turnover, i.e. an increasing in photosynthetic carbon fixation followed by an increasing subsequent fractional organic carbon burial, and that related to bio-radiation such as increasing algae, bacteria, and original creatures productivity in biomass. These secular variations are interpreted to reflect perturbations of the regional carbon cycle, specifically changes in the fractional burial of organic carbon, and discuss the relationship between Gaojiashan biota and paleoenvrionmental variation.     

Variations in Stable Carbon Isotopic Composition of n-Alkanes from Ordovician and Triassic-Derived Oils in Lunnan Oilfield, Tarim Basin, NW China： Global Paleoenvironmental Constraints

Molecular stable carbon isotope technique was employed to study well-sourced crude oils collected from a single drilling well and from the entire Lunnan oilfield, Tarim Basin, NW China. The stable carbon isotopic composition of n-alkanes from crude oils showed that Ordovi-clan-derived oils are enriched in ^13C and Triassic-derived oils are depleted in ^13C. This is consistent with the distribution and evolution trend of stable carbon isotope ratios in crude oils/organic matter from all over the world in geological history (Stahl, 1977; Andrusevich et al. ,1998). An extensive survey of literature indicates that, except for thermal maturity, organic matter input and depositional environment, paleoenvironmental background is another key factor that affects the stable carbon isotopic composition of Ordovician- and Triassic-derived crude oils. The results showed that gas chromatographic-isotope ratio mass spectrometry ( GC-C-IRMS), combining with biogeoehemical evolution of organic matter in geological history, may be a powerful tool in refining oil/oil, oil/source correlations in multi-age, multi-source petroliferous basins like Tarim.     

Stable Carbon Isotopic Compositions of Methylated-MTTC in Crude Oils from Saline Lacustrine Depositional Environment: Source Implications

Significantly high abundant methyl-MethylTrimethylTridecylChromans (MTTCs) have been detected in aromatic hydrocarbon fractions in crude oils from the Jizhong Depression and Jianghan Basin. The distribution of these compounds is dominated by methyl-MTTC and dimethyl-MTTC series, which indicate diagenetic products of a hypersaline depositional environment in the early stage and show a low degree of methylation. The occurrence of significantly high abundant methyl-MTTC depends mainly on good preservation conditions with a strongly reductive, hypersaline and water-columned depositional environment and subsequent non-intensive diagenetic transformations. The stable carbon isotopic compositions of the methyl-MTTCs and dimethyl-MTTCs in two samples are far different from the stable carbon isotopic composition of C30 hopane of apparent bacteria biogenesis (up to 4.11‰ and 5.75‰, respectively). This obviously demonstrates that the methyl-MTTC and dimethyl-MTTCs cannot be of bacteria origin, which is different from the previous point of view about non-photosynthetic bacteria products or possible bacteria-reworked products. On the contrary, the stable carbon isotopic compositions of methyl-MTTC and dimethyl-MTTCs in the two samples were similar to that of the same carbon-numbered n-alkanes (nC27-nC28-nC29), which indicates that they share the same source origin. Especially in the crude oil from the Zhao61 well, stable carbon isotopic compositions are also similar to that of the same carbon-numbered steranes with ααα-20R isomer (mostly less than 0.4‰). In consideration of the results of previous studies on saline lake ecological sedimentation, the authors hold that the methyl-MTTC and dimethyl-MTTCs in the saline lake sediments should be of algal biogenesis origin.     

Origin of natural gases and their differences between the eastern and western parts of central Tarim Basin

The origin of natural gases in central Tarim Basin is very complicated and there has been no definite conclusion in this aspect. Based on the results of systematic research on their composition and carbon isotopic characteristics, natural gases in central Tarim Basin are composed mainly of hydrocarbon gas, Ordovician natural gas with the characteristics of crude oil-cracking gas, and Carboniferous natural gas not only originating from kerogen cracking, but also from oil cracking. There are significant differences in composition and carbon isotope of natural gases between the eastern and western areas. The causes for the differences in geochemical characteristics of natural gases are presented as follows: different thermal evolution degrees of organic matter. Natural gases in the western region may have generated from the Middle- Upper Ordovician source rocks, and natural gases in the eatern region may be derived from the Cambrian source rocks, which entered into high to over mature stages; the gases migrated from west to east and caused the different compositional and carbon isotopic characteristics of natural gases; difference in the strength of thermal sulfate reduction between the eastern and western parts, with the reduction in the eastern part being stronger than that in the western part.     

东海泥质区单体正构烷烃的碳同位素组成及物源分析 *

利用气相色谱(GC)和气相色谱/同位素比值质谱(GC/IRMS)对东海近岸泥质区、济州岛西南泥质区和冲绳海槽北部表层沉积物中正构烷烃的单体碳同位素组成及分布进行了分析。结果显示东海不同泥质区典型海洋藻类源正构烷烃C₁₉同位素组成基本相似,在-27.4 ‰ ~-28.0 ‰ 之间,平均为-27.7 ‰ 。典型海洋水生植物源C₂₃同位素组成在-28.5 ‰ ~-31.6 ‰ 之间,平均为-30.5 ‰ ,碳同位素组成从近岸泥质区到冲绳海槽北部逐渐变重,表明海槽区与陆架区海洋水生植物种类有所不同。陆架区长链正构烷烃(C₂₅~C₃₁)部分随着碳数的增加,其同位素组成逐渐变轻,但海槽区这一变化不大,显示陆架区的陆源高等植物蜡具有相似的物源,而冲绳海槽北部由于黑潮主干区和黑潮分支(对马暖流)对陆架沉积物进入深海的控制性阻隔作用,其物源与陆架区区别较大。现代输入东海的陆源植物以C₃植物为显著优势,C₃植物对近岸泥质区北部、近岸泥质区南部、远端济州岛西南泥质区和冲绳海槽北部陆源植物的贡献分别为83 % ,95 ％,75 % 和70 % 。     

干旱-半干旱区兰州兴隆山现代森林典型植被和土壤中类脂物分子特征及其意义

利用GC－MS对西北干旱区-半干旱区兰州兴隆山森林区典型植被与现代土壤样品中可抽提的类脂物进行了系统分析,检测出包括正构烷烃和α正构脂肪酮等一系列类脂物分子化石。在未进行族分离的情况下,检出兴隆山现代森林木本植物的正构烷烃以C₂₇或C₂₉为主峰,草本植物则以C₃₁为主峰;  土壤样品中均保留有很强的、几乎均势的C₂₇,C₂₉和C₃₁信号; α正构脂肪酮具有明显的奇碳优势,植物中以C₂₃,C₂₅或C₂₉为主峰,土壤样品以C₂₇或C₂₉为主峰;  其反映的信息是植被与微生物共同作用的结果。本研究为理解现代土壤和古土壤中类脂物所指示的植被信息、进一步探讨类脂物分子在植被(有机质)-微生物-土壤-湖泊沉积体系中存在与相互转换关系这一基础理论问题提供了科学资料。同时,为分子化石分析方法的改进和不同处理过程所得数据之间的对比和科学解释提供资料。     

Hydrogen isotope ratios of recent lacustrine sedimentary n-alkanes record modern climate variability

Hydrogen isotope ratios were measured on n-alkanes (n-C₁₂ to n-C₃₁) extracted from recent lake surface sediments along a N-S European transect to test if modern climate variability is recorded in these biomarkers. δD values of the n-alkanes are compared to δD values of meteoric water from the IAEA-GNIP database spanning a range from −119‰ in northern Sweden to −41‰ in southern Italy, to lake water δD values, and to mean annual temperatures, varying between −2.0°C in the north and 13.7°C in the south.δD values of the short-chained n-alkanes n-C₁₂ to n-C₂₀, excluding algal derived n-C₁₇ and n-C₁₉, are higher in the north and lower in the south. The isotopic fractionation ε for hydrogen between meteoric water and the short-chained n-alkanes is increasing from N to S by more than 100‰ and is significantly correlated to mean annual temperature for n-C₁₆ and n-C₁₈. This suggests that these n-alkanes may originate from a different source in the northern lakes, possibly due to petroleum contamination, or are synthesized using a different biochemical pathway.The n-C₁₇ and n-C₁₉ alkanes of algal origin, the n-C₂₁ and n-C₂₃ alkanes originating from water plants, and the long-chain n-alkanes n-C₂₅, n-C₂₇, n-C₂₉, and n-C₃₁ of terrestrial origin, clearly correlate with δD values of meteoric water, lake water, and mean annual temperature, indicating that they excellently record the δD value of meteoric water. The mean hydrogen isotope fractionation ε_C17/w of −157‰ (SD = 13) between n-C₁₇ and meteoric water is fairly constant over the wide range of different climates and lake environments, suggesting only minor influence of environmental factors on this biochemical fractionation. This suggests that δD values of n-C₁₇ are suitable to reconstruct the isotopic composition of source water. The mean fractionation between the long-chain n-alkanes and water is −128‰ (SD = 12). The mean difference of 31‰ between both ε values is likely due to evaporative enrichment of deuterium in the leaf water. If this is the only influence on the enrichment, the difference between the δD values of terrestrial and aquatic compounds might be suitable to reconstruct terrestrial evapotranspiration of the lake environment.     

Unusual N—Alkane Distributions in Extracts from Marine Carbonate Rocks at High Levels of Maturity and Overmaturity

N-alkanes in extracts from possible carbonate source rocks of the Lower Ordovician Majiagou Formation in the central gas field of the Shanganning Basin and the Upper Sinian Dengying Formation in the Weiyuan gas field of the Sichuan Basin, are characterized by bimodal distributions with the dominant carbon numbers in the range C₁₇-C₂₁ and C₂₅-C₂₉. In most samples, the lower carbon number components are present in greater abundance than the higher carbon number ones. Most samples contain significant concentrations of waxy hydrocarbons (C₂₂₊) with C_21-/C₂₂₊ ratios between 0.50 to 3. 16, and an average value of 1. 34. The n-alkanes in extracts of outcrops and shallow core samples of Upper Proterozoic and Lower Palaeozoic carbonate rocks in the western and southern parts of the North China Basin are of unimodal distributions dominated by n-alkanes maximizing in the C₂₅-C₂₉ range. These extracts have very high concentrations of waxy hydrocarbons with C_21-/C₂₂₊ ratios all < 1. 0, ranging from 0. 14 to 0. 90 and averaging 0. 36. All of the extracts have a marked odd/even predominance in the high molecular weight n-alkane range regardless of whether they are from shallow or deep cores or out-crop samples. Simulation experiments were performed using typical sapropelic-type kerogens from the immature Sinian Lower Xiamalin Formation carbonate-rich shales collected at Jixian, Hebei Province, North China Basin, and the contemporary microplanktonic blue-green algaeSpirulina subsala. Results indicate that the unusual distribution of n-alkanes in the extracts of Upper Proterozoic and Lower Palaeozoic carbonate rocks possibly originated from algae in the source rocks at high levels of maturity and overmaturity. This research project was financially supported by the Chinese Academy of Sciences (Grant No. KZCX2-111 ).     

准噶尔盆地液态烃分子碳同位素组成特征及其应用

文章报导了准噶尔盆地不同地区、不同产层原油和烃源岩样品中正构烷烃和类异成二烯烃碳同位素组成特征。在ｎＣ₁₁－ｎＣ₃₄之间，保罗系湖沼相成因的原油，正构烷烃δ13Ｃ值大部分分布在－２７．０‰──３２．４‰之间，比海相地层的原油重，具有富集13Ｃ的特征。ⅡＡ型烃源岩产出原油的单烃δ13Ｃ值比ⅡＢ型的轻，相对富集12Ｃ。碳源组成相同的原油在正构烷烃和类异成二烯烃碳同位素组成上，有相似的分布范围和较为一致的总体变化趋势，因此单烃碳同位素组成可用于油－油对比和油－源对比中。     

Origin and depositional environments of source rocks and crude oils from Niger Delta Basin: Carbon isotopic evidence

Thirty-nine crude oils and twenty-one rock samples from Niger Delta Basin, Nigeria have been characterized based on their isotope compositions by elemental analysis-isotope ratio mass spectrometry and gas chromatography-isotope ratio mass spectrometry. The bulk carbon isotopic values of the whole rock extracts, saturate and aromatic fractions range from –28.7‰ to –26.8‰, –29.2‰ to –27.2 ‰ and –28.5 ‰ to –26.7 ‰, respectively while the bulk carbon isotopic values of the whole oils, saturate and aromatic fractions range from –25.4 ‰ to –27.8 ‰, –25.9 ‰ to –28.4 ‰ and –23.5 ‰ to –26.9 ‰, respectively. The average carbon isotopic compositions of individual alkanes (nC₁₂-nC₃₃) in the rock samples range from –34.9‰ to –28.2‰ whereas the average isotopic values of individual n-alkanes in the oils range from –31.1‰ to –23.8‰. The δ¹³C isotope ratios of pristane and phytane in the rock samples range from –29.2 ‰ to –28.2 ‰ and –30.2 ‰ to –27.4 ‰ respectively while the pristane and phytane isotopic values range from –32.1‰ to –21.9‰ and –30.5‰ to –26.9‰, respectively. The isotopic values recorded for the samples indicated that the crude oils were formed from the mixed input of terrigenous and marine organic matter and deposited under oxic to sub-oxic condition in lacustrine-fluvial/deltaic environments. The stable carbon isotopic compositions were found to be effective in assessing the origin and depositional environments of crude oils in the Niger Delta Basin.     

Influence of diet on the distribution of carbon isotopes in animals

The influence of diet on the distribution of carbon isotopes in animals was investigated by analyzing animals grown in the laboratory on diets of constant carbon isotopic composition.The isotopic composition of the whole body of an animal reflects the isotopic composition of its diet, but the animal is on average enriched in δ¹³C by about 1‰ relative to the diet. In three of the four cases examined, the ¹³C enrichment of the whole body relative to the diet is balanced by a ¹³C depletion of the respired CO₂. The isotopic relationships between the whole bodies of animals and their diets are similar for different species raised on the same diet and for the same species raised on different diets. However, the δ¹³C values of whole bodies of individuals of a species raised on the same diet may differ by up to 2‰. The relationship between the ¹³C/¹²C ratio of a tissue and the ¹³C/¹²C ratio of the diet depends both on the type of tissue and on the nature of the diet. Many of the isotopic relationships among the major biochemical fractions, namely the lipid, carbohydrate and protein fractions, are qualitatively preserved as diet carbon is incorporated into the animal. However, the difference between the δ¹³C values of a biochemical fraction in an animal and in its diet may be as large as 3‰. The δ¹³C values of the biochemical components collagen, chitin and the insoluble organic fraction of shells, all of which are often preserved in fossil material, are related to the isotopic composition of the diet.These results indicate that it will be possible to perform dietary analysis based on the determination of the ¹³C/¹²C ratio of animal carbon. Analysis of the total animal carbon will in most cases provide a better measure of diet than the analysis of individual tissues, biochemical fractions, or biochemical components. The limits of accuracy of this method will generally restrict its application to situations in which the diet is derived from sources with relatively large differences in their δ¹³C values, such as terrestrial vs aquatic organisms or C₃ vs C₄ plants. The method should be applicable to fossil as well as to living material.     

Latest Devonian to earliest Carboniferous conodont and carbon isotope stratigraphy of a shallow‐water sequence in South China

To improve regional and intercontinental correlation of the uppermost Devonian–lowermost Carboniferous, we examined the conodont faunas and carbon isotopic records of the Tangbagou Formation in the Qilinzhai section, southern Guizhou, South China. The Tangbagou Formation is a succession of mixed carbonate–siliciclastic rocks that accumulated on a shallow‐water platform under normal marine conditions. Seven conodont zones for shallow‐water biofacies in South China, the Cl. gilwernensis–Cl. unicornis Zone, the Po. spicatus Zone, the Si. homosimplex Zone, the Si. sinensis Zone, the Si. eurylobata Zone, the Ps. multistriatus Zone and the Po. co. porcatus Zone in ascending order, are recognized in the Tangbagou Formation. Although apparently limited in its value for global correlation, this conodont zonation is more applicable to shallow‐water biofacies in South China. Carbonate samples have yielded carbon isotopic signatures consistent with those recorded in Euroamerica sections, in particular showing four distinct characteristics: (1) the peak values of Hangenberg Carbon Isotope Excursion (HICE) during the latest Devonian, (2) a minor positive shift (P1) in the Si. homosimplex Zone during the early Tournaisian, (3) a second minor positive shift (P2) in the Si. sinensis Zone and (4) the middle Tournaisian Carbon Isotope Excursion (TICE) in the middle part of the Tangbagou Formation. The similarity in peak values (~5.5‰) and magnitude of TICE for the Qilinzhai and Belgian sections indicates that the Euro‐asia δ¹³C_carb trends may reflect the changes in global mean ocean δ¹³C_DIC, rather than having been overprinted by local carbon cycling. Integration of conodont biostratigraphy and δ¹³C stratigraphy provides a powerful tool for stratigraphic correlation. Copyright © 2015 John Wiley & Sons, Ltd.     

柴达木盆地北缘原油中单体正构烷烃的碳、氢同位素组成研究

以柴达木盆地北缘不同构造带代表性原油作为研究对象,采用GC-TC-IRMS技术对原油中正构烷烃单体碳、氢同位素进行测定。利用样品正构烷烃单体碳、氢同位素组成特征及分布模式,进行原油成因类型划分和对比分析。研究结果表明,正构烷烃可溶有机质的δ13C分布在-36‰～-25‰,δD分布在-180‰～-110‰。对比发现,不同构造带原油中正构烷烃单体碳、氢同位素组成特征上存在着比较明显的差别。以-30‰（δ13C）和 -140‰（δD）作为分界,结合同位素曲线的分布型式,可以划分为不同的分布模式判识生烃母质和沉积环境。     

The influence of hydrocarbon expulsion on carbon isotopic compositions of individual n-alkanes in pyrolysates of selected terrestrial kerogens

Expulsion of petroleum from source rock is a complex part of the entire migration process. There exist fractional effects on chemical compositions in hydrocarbon expulsion. Does the carbon isotopic fractionation occur during expulsion and to what extent? Here the influence of hydrocarbon expulsion on carbon isotopic compositions of individual n-alkanes from pyrolysates of selected terrestrial kerogens from Tuha basin and Fushun, Liaoning Province of China has been experimentally studied. The pyrogeneration-expulsion experiments were carried out under semi-closed system. The carbon isotopic compositions of individual n-alkanes were measured by GC-IRMS. The main conclusions are as follows. First, there is carbon isotopic fractionation associated with hydrocarbon expulsion from Type III kerogens in Tuha Basin. There exist differences of carbon isotopic compositions between the unexpelled n-alkanes and expelled n-alkanes from Tuha desmocollinite and Tuha mudstone. Second, there is almost no carbon isotopic fractionation associated with hydrocarbon expulsion from Type II kerogens in Fushun and Liaohe Basin. Third, carbon isotopic fractionation in hydrocarbon expulsion should be considered in making oil-source correlation of Type III kerogens at least in the Tuha Basin. Further studies need to be carried out to determine whether this is true in other basins. Fourth, oil and source at different maturity levels cannot be correlated directly for Type III kerogens since the carbon isotopic compositions of expelled hydrocarbons at different temperatures are different. The expelled hydrocarbons are usually lighter (depleted in ¹³C) than the hydrocarbons remaining in the source rock at the same maturity.